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Merck

H20202

4-Hydroxybenzophenone

98%

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About This Item

Linear Formula:
HOC6H4COC6H5
CAS Number:
Molecular Weight:
198.22
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
214-507-1
Beilstein/REAXYS Number:
777776
MDL number:
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Quality Level

assay

98%

mp

132-135 °C (lit.)

SMILES string

Oc1ccc(cc1)C(=O)c2ccccc2

InChI

1S/C13H10O2/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,14H

InChI key

NPFYZDNDJHZQKY-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

General description

4-Hydroxybenzophenone is characterized by its ability to absorb UV radiation and convert it into lower-energy radiation. This property makes it an effective photostabilizer. Its molecular structure features two aromatic rings connected by a carbonyl group, allowing for strong π-π stacking interactions, which enhance its stability and efficacy in polymer matrices. Incorporating 4-Hydroxybenzophenone into polymer matrices increases the longevity and performance of materials used in outdoor applications, such as coatings and plastics.

Application

4-Hydroxybenzophenone can be used:
  • As a photoinitiator to synthesize fluorescent triblock copolymer micelles for targeted release of cancer drugs and intracellular bioimaging. It facilitates controlled release, improving therapeutic efficacy while minimizing side effects.
  • As a photoacid catalyst for ring opening polymerization of lactones to prepare biodegradable polyesters.
  • As a precursor to synthesize functional copolymer for fabrication of nanostructured transparent metal electrodes for flexible optoelectronic devices.


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pictograms

Health hazard

signalword

Warning

hcodes

Hazard Classifications

Aquatic Chronic 3 - STOT RE 2

target_organs

Liver,Kidney

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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